Key result
Cardiometabolic state correlates with white-matter hyperintensities and mediates their link to ventricular and EEG changes.
Why the study?
The influence of systemic cardiometabolic and vascular markers on brain structure and function remains less understood.
Does cardiometabolic state correlate with neurovascular burden and brain structure/function in healthy aging individuals?
Cross-Sectional (n=196)
Does cardiometabolic state correlate with neurovascular burden and brain structure/function in healthy aging individuals?
Cardiometabolic state, measured by an allostatic load index, is significantly associated with neurovascular burden, ventricular enlargement, and altered EEG activity in aging.
No immediate clinical implications for healthy aging; leaves open causal links and need for longitudinal confirmation.
• Cardiometabolic status -as measured by the Allostatic load index (ALI)- correlates with neurovascular burden, as well as structural and functional signatures of the aging brain. • Cardiometabolic status links ventricular enlargement but not hippocampal atrophy with neurovascular burden. • EEG spectral exponent flattening and not alpha power -two functional signatures of the ageing brain- correlate with cardiometabolic state and neurovascular burden. • Cardiometabolic status fully mediates the relationship between neurovascular burden-related inflammation -as indicated by ventricular enlargement- and flattened EEG spectral exponent • Our findings suggest neuroinflammatory pathways explaining linking cardiometabolic health, WMHs, and EEG changes in ageing. Aging affects brain structure and function alongside metabolic and vascular processes leading to energetic impairments. While local neurometabolic dysfunction in aging is well-documented, the influence of systemic cardiometabolic and vascular markers on brain structure and function remains less understood. We examine the link between cardiometabolic dysfunction (measured by an allostatic load index) and neurovascular burden (measured by white matter hyperintensities) with brain changes, including ventricular and hippocampal volume, as well as EEG activity, through aging. Analyzing data from 196 healthy individuals across ages (20-75 years), we found a significant positive correlation between allostatic load index and white-matter hyperintensities, irrespective of age. White matter hyperintensities are also positively linked with ventricular enlargement, but not hippocampal atrophy. The allostatic load index mediated the relationship between white-matter hyperintensities and ventricular volume. Regarding brain function, changes in the spectral aperiodic exponent but not periodic alpha power were linked to white matter hyperintensities and the allostatic load index. Such index mediated the relationship between spectral aperiodic exponent and white matter hyperintensities. Thus, findings suggest that the cardiometabolic state, as measured by an allostatic load index, plays a crucial role in brain health in aging, particularly influencing ventricular enlargement and increased aperiodic activity.
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Franco-O’Byrne et al. (2025) conducted a cross-sectional in Healthy aging (n=196). Allostatic load index (cardiometabolic status) was evaluated on Correlation between allostatic load index, white-matter hyperintensities, brain volume, and EEG activity. Cardiometabolic state, measured by an allostatic load index, significantly correlated with white-matter hyperintensities and mediated their relationship with ventricular enlargement and EEG changes.
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